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基于聚多巴胺点的荧光纳米开关用于人血清和活细胞中谷氨酸和铝的可逆识别

Polydopamine Dots-Based Fluorescent Nanoswitch Assay for Reversible Recognition of Glutamic Acid and Al in Human Serum and Living Cell.

机构信息

Key Laboratory of Flexible Electronics (KLOFE), Institute of Advanced Materials (IAM), Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM) , Nanjing Tech University (NanjingTech) , 30 South Puzhu Road , Nanjing 211816 , China.

State Key Laboratory of Chemo/Biosensing and Chemometrics , Hunan University , Changsha 410082 , China.

出版信息

ACS Appl Mater Interfaces. 2018 Oct 24;10(42):35760-35769. doi: 10.1021/acsami.8b12087. Epub 2018 Oct 11.

Abstract

We developed a facile and feasible fluorescent nanoswitch assay for reversible recognition of glutamate (Glu) and Al in human serum and living cell. The proposed nanoswitch assay is based on our recently developed method for controlled synthesis of fluorescent polydopamine dots (PDADs) at room temperature with dopamine as the sole precursor. The fluorescence of nanoswitch assay could be quickly and efficiently quenched by Glu (turn-Off), and the addition of Al could recover the fluorescence of the PDADs-Glu system (turn-On). Meanwhile, the reversible recognition of Glu and Al in this nanoswitch system was stable after three cycles. Additionally, the system displayed excellent performance for Glu and Al determination with a low detection limit of 0.12 and 0.2 μM, respectively. Moreover, PDADs are successfully applied to determine Glu and monitor Al in human serum. Noteworthy, the nanoswitch assay is transported into HepG2 cells and realized "Off" detection of Glu and "On" sensing Al in the living cells. Therefore, this PDADs-based nanoswitch assay provides a strategy to develop reversible recognition biosensors for intracellular and external molecular analysis.

摘要

我们开发了一种简便可行的荧光纳米开关分析方法,用于可逆识别人血清和活细胞中的谷氨酸(Glu)和 Al。所提出的纳米开关分析方法基于我们最近开发的方法,即在室温下使用多巴胺作为唯一前体来控制合成荧光聚多巴胺点(PDADs)。纳米开关分析的荧光可以被 Glu 快速有效地猝灭(关闭),而 Al 的加入可以恢复 PDADs-Glu 体系的荧光(打开)。同时,该纳米开关系统中 Glu 和 Al 的可逆识别在三个循环后仍然稳定。此外,该系统在 Glu 和 Al 的测定中表现出优异的性能,检测限分别低至 0.12 和 0.2 μM。此外,PDADs 成功应用于测定人血清中的 Glu 并监测 Al。值得注意的是,该纳米开关分析被运用于 HepG2 细胞,并实现了 Glu 的“关闭”检测和细胞内 Al 的“开启”感应。因此,基于 PDADs 的纳米开关分析为开发用于细胞内和外部分子分析的可逆识别生物传感器提供了一种策略。

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